Literature DB >> 7977364

Parental origin effects, genome imprinting, and sex-ratio distortion: double or nothing?

C Sapienza.   

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Year:  1994        PMID： 7977364      PMCID： PMC1918446     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  13 in total

1.  Unusual segregation of cystic fibrosis alleles.

Authors:  A Kitzis; J C Chomel; A Haliassos; L Tesson; J C Kaplan; J Feingold; G Giraud; A Lable; B Dastugue; V Dumur
Journal:  Nature       Date:  1988-11-24       Impact factor: 49.962

2.  Is there a relationship between sex of cystic fibrosis carriers and sex ratio of their offspring?

Authors:  F Gloria-Bottini; M Antonelli; S Quattrucci; E Cardi; E Bottini
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

3.  Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC.

Authors:  H Donis-Keller; S Dou; D Chi; K M Carlson; K Toshima; T C Lairmore; J R Howe; J F Moley; P Goodfellow; S A Wells
Journal:  Hum Mol Genet       Date:  1993-07       Impact factor: 6.150

4.  Cystic fibrosis allele frequency, sex ratio anomalies and fertility: a new theory for the dissemination of mutant alleles.

Authors:  D J Pritchard
Journal:  Hum Genet       Date:  1991-10       Impact factor: 4.132

5.  Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A.

Authors:  L M Mulligan; J B Kwok; C S Healey; M J Elsdon; C Eng; E Gardner; D R Love; S E Mole; J K Moore; L Papi
Journal:  Nature       Date:  1993-06-03       Impact factor: 49.962

6.  Parent-of-origin effects in multiple endocrine neoplasia type 2B.

Authors:  K M Carlson; J Bracamontes; C E Jackson; R Clark; A Lacroix; S A Wells; P J Goodfellow
Journal:  Am J Hum Genet       Date:  1994-12       Impact factor: 11.025

7.  Interspecific backcross mice show sex-specific differences in allelic inheritance.

Authors:  L D Siracusa; W G Alvord; W A Bickmore; N A Jenkins; N G Copeland
Journal:  Genetics       Date:  1991-08       Impact factor: 4.562

8.  A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma.

Authors:  R M Hofstra; R M Landsvater; I Ceccherini; R P Stulp; T Stelwagen; Y Luo; B Pasini; J W Höppener; H K van Amstel; G Romeo
Journal:  Nature       Date:  1994-01-27       Impact factor: 49.962

9.  Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B.

Authors:  K M Carlson; S Dou; D Chi; N Scavarda; K Toshima; C E Jackson; S A Wells; P J Goodfellow; H Donis-Keller
Journal:  Proc Natl Acad Sci U S A       Date:  1994-02-15       Impact factor: 11.205

10.  Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC.

Authors:  L M Mulligan; C Eng; C S Healey; D Clayton; J B Kwok; E Gardner; M A Ponder; A Frilling; C E Jackson; H Lehnert
Journal:  Nat Genet       Date:  1994-01       Impact factor: 38.330
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  7 in total

1.  Age and sex based genetic locus heterogeneity in type 1 diabetes.

Authors:  A D Paterson; A Petronis
Journal:  J Med Genet       Date:  2000-03       Impact factor: 6.318

Review 2.  Paternal factors and schizophrenia risk: de novo mutations and imprinting.

Authors:  D Malaspina
Journal:  Schizophr Bull       Date:  2001       Impact factor: 9.306

Review 3.  Rates of spontaneous mutation.

Authors:  J W Drake; B Charlesworth; D Charlesworth; J F Crow
Journal:  Genetics       Date:  1998-04       Impact factor: 4.562

Review 4.  Multiple endocrine neoplasia type 2B (mucosal neuroma syndrome, Wagenmann-Froboese syndrome).

Authors:  P J Morrison; N C Nevin
Journal:  J Med Genet       Date:  1996-09       Impact factor: 6.318

5.  Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23.

Authors:  B E Baysal; J E Farr; W S Rubinstein; R A Galus; K A Johnson; C E Aston; E N Myers; J T Johnson; R Carrau; S J Kirkpatrick; D Myssiorek; D Singh; S Saha; S M Gollin; G A Evans; M R James; C W Richard
Journal:  Am J Hum Genet       Date:  1997-01       Impact factor: 11.025

6.  Prevalence and parental origin of de novo RET mutations in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma. Le Groupe d'Etude des Tumeurs a Calcitonine.

Authors:  I Schuffenecker; N Ginet; D Goldgar; C Eng; B Chambe; A Boneu; C Houdent; D Pallo; M Schlumberger; C Thivolet; G M Lenoir
Journal:  Am J Hum Genet       Date:  1997-01       Impact factor: 11.025

7.  Paternal germline origin and sex-ratio distortion in transmission of PTPN11 mutations in Noonan syndrome.

Authors:  Marco Tartaglia; Viviana Cordeddu; Hong Chang; Adam Shaw; Kamini Kalidas; Andrew Crosby; Michael A Patton; Mariella Sorcini; Ineke van der Burgt; Steve Jeffery; Bruce D Gelb
Journal:  Am J Hum Genet       Date:  2004-07-09       Impact factor: 11.025
  7 in total

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